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Synthesis and Biological Evaluation of Novel Substituted 1,3,4-thiadiazole and 2,6-di aryl substituted imidazo 2,1-udb 1,3,4thiadiazole Derivatives

机译:新型取代的1,3,4-噻二唑和2,6-二芳基取代的咪唑2,1- ud的合成及生物评价b 1,3,4噻二唑衍生物

摘要

A new series of N-[5-(4-(alkyl/aryl)-3-nitro-phenyl)-[1,3,4-thiadiazol-2-yl]-2,2-dimethyl-propionamide 4(ael) and 6-(4-Methoxy-phenyl)-2-(4-alkyl/aryl)-3-nitro-phenyl)-Imidazo [2,1-b] [1,3,4] thiadiazole 6(ael) were synthesized starting from 5-(4-Fluoro-3-nitro-phenyl)-[1,3,4] thiadiazole-2-ylamine. The synthesized compounds were characterized by IR, NMR, mass spectral and elemental analysis. All the compounds were tested for antibacterial and antifungal activities. The antimicrobial activities of the compounds were assessed by well plate method (zone of inhibition). Compounds 4a,4c and 6e,6g displayed appreciable activity at the concentration 0.5 - 1.0 mg/mL.
机译:新系列的N- [5-(4-(烷基/芳基)-3-硝基-苯基)-[1,3,4-噻二唑-2-基] -2,2-二甲基丙酰胺4(ael)合成了6-(4-甲氧基-苯基)-2-(4-烷基/芳基)-3-硝基-苯基)-咪唑[2,1-b] [1,3,4]噻二唑6(ael)从5-(4-氟-3-硝基-苯基)-[1,3,4]噻二唑-2-基胺开始。合成的化合物通过IR,NMR,质谱和元素分析进行​​表征。测试所有化合物的抗菌和抗真菌活性。通过孔板法(抑制区)评估化合物的抗微生物活性。化合物4a,4c和6e,6g在浓度为0.5-1.0 mg / mL时显示出明显的活性。

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